A new preparation of furo-2,3b furans, and conformational studies by 2D NMR.
β Scribed by M. Jalali; G. Boussac; J.-Y. Lallemand
- Publisher
- Elsevier Science
- Year
- 1983
- Tongue
- French
- Weight
- 194 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Perhydro furo-2,3-b furan derivatives have been prepared by iodocyclisation of unsaturated lactols. Structure and conformation have been studied by high resolution "COSY" 20 NMR.
π SIMILAR VOLUMES
Fused ring cyclic ketals are frequently encountered in natural products . Furo-2,3bfurans or pyrans, for example, are present in many natural insect antifeeding compounds and
Perhydrofuro-2,3b furans have been prepared in high yield by radical cyclisation of unsaturated bromo acetals. Their transformation into tetrahydro derivatives is described along with a radical annelation to 2,3-dihydrofurans by tributyltin iodoacetate.